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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Drd1a-cre)AGsc
transgene insertion A, Gunther Schutz
MGI:3761818
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Nr3c1tm2Gsc/Nr3c1tm2Gsc
Tg(Drd1a-cre)AGsc/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:3852119
cn2
Drd2tm3.1Ebo/Drd2tm3.1Ebo
Tg(Drd1a-cre)AGsc/0
involves: 129S2/SvPas * C57BL/6 * FVB/N MGI:5431883
cn3
Chrm4tm2.1Jwe/Chrm4tm2.1Jwe
Tg(Drd1a-cre)AGsc/0
involves: 129S6/SvEvTac * C57BL/6 * FVB/N MGI:4442324


Genotype
MGI:3852119
cn1
Allelic
Composition
Nr3c1tm2Gsc/Nr3c1tm2Gsc
Tg(Drd1a-cre)AGsc/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nr3c1tm2Gsc mutation (1 available); any Nr3c1 mutation (35 available)
Tg(Drd1a-cre)AGsc mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• Anxiety-related behavior, basic motor processes (movement, coordination), and associative learning are not impaired in mutants
• mice show profoundly decreased cocaine self-administration; acquistion of cocaine self-administration is similar to controls but dose-response is decreased indicating a lower reinforcing efficacy of cocaine

nervous system
• spontaneous firing rate of dopamine neurons is highly reduced in ventral tegmental area (VTA)

homeostasis/metabolism
N
• circulating glucocorticoid levels are normal under basal and stress conditions
• anxiety-related behaviors are not altered compared to controls indicating behavioral changes are specific to cocaine reinforcement




Genotype
MGI:5431883
cn2
Allelic
Composition
Drd2tm3.1Ebo/Drd2tm3.1Ebo
Tg(Drd1a-cre)AGsc/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Drd2tm3.1Ebo mutation (0 available); any Drd2 mutation (70 available)
Tg(Drd1a-cre)AGsc mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice treated with cocaine exhibit a blunted hyperactivity response compared with control mice
• mice fail to exhibit catalepsy induced by haloperidol compared with control mice
• on a rotarod
• in the home cage and open field
• in mice fed cocaine

nervous system
N
• mice exhibit normal dopamine levels
• neurons exhibit smaller relative peak amplitudes compared with control neurons

homeostasis/metabolism
• dopamine overflow evoked by a single stimulus in the dorsal striatum (DSt) is decreased compared to in control mice
• quinpirole-treated mice exhibit attenuated inhibition of dopamine overflow compared with control mice
• mice exhibit lower AMP evoked dopamine release compared with control mice
• however, mice exhibit normal dopamine reuptake
• mice fail to exhibit catalepsy induced by haloperidol compared with control mice
• mice treated with quinpirole exhibit less of a decreased in locomotion compared with control mice




Genotype
MGI:4442324
cn3
Allelic
Composition
Chrm4tm2.1Jwe/Chrm4tm2.1Jwe
Tg(Drd1a-cre)AGsc/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Chrm4tm2.1Jwe mutation (0 available); any Chrm4 mutation (35 available)
Tg(Drd1a-cre)AGsc mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the inhibitory effect of carbachol, a hydrolytically stable ACh analog, is not observed in striatal membranes exposed to the D1 receptor agonist, SKF82958.

behavior/neurological
• enhanced activity at the highest dose (30 ug/kg) of SKF82958, a D1 receptor agonist
• significantly more active following a high dose (2 mg/kg) of amphetamine
• develop enhanced amphetamine induced behavioral sensitization
• significantly more active following exposure to a high dose (10 mg/kg) of cocaine
• develop enhanced cocaine induced behavioral sensitization
• haloperidol induced and risperidone induced catalepsy are attenuated
• enhanced activity at the highest dose of SKF82958, a D1 receptor agonist
• enhanced activity at high doses of cocaine (10 mg/kg) or amphetamine (2 mg/kg)
• haloperidol induced and risperidone induced catalepsy are attenuated

homeostasis/metabolism
• basal dopamine efflux in the nucleus accumbens of is increased two- to three-fold
• absolute amphetamine-induced dopamine efflux was significantly enhanced at the 120 min time point, as compared to control mice
• however, the relative percent increase induced by amphetamine exposure is not different from controls





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory